Package 0009-0011-04

Brand: solu-cortef

Generic: hydrocortisone sodium succinate
NDC Package

Package Facts

Identity

Package NDC 0009-0011-04
Digits Only 0009001104
Product NDC 0009-0011
Product ID 0009-0011_8512044a-4a54-4634-bb97-9e20126adc61
Description

25 VIAL, SINGLE-DOSE in 1 CARTON (0009-0011-04) / 2 mL in 1 VIAL, SINGLE-DOSE (0009-0011-03)

Marketing

Marketing Status
Marketed Since 1955-04-27
Brand solu-cortef
Generic hydrocortisone sodium succinate
Sample Package No

Linked Drug Pages (1)

Solu-Cortef ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["INTRAMUSCULAR", "INTRAVENOUS"], "spl_id": "8512044a-4a54-4634-bb97-9e20126adc61", "openfda": {"upc": ["0300090016128", "0300090013059", "0300090005016"], "unii": ["50LQB69S1Z"], "rxcui": ["105398", "238755", "1738586", "1738589", "1738590", "1738592", "1738594", "1738596"], "spl_set_id": ["65eefd58-b166-4d71-ade6-45c8fdf86922"], "manufacturer_name": ["Pharmacia & Upjohn Company LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "25 VIAL, SINGLE-DOSE in 1 CARTON (0009-0011-04)  / 2 mL in 1 VIAL, SINGLE-DOSE (0009-0011-03)", "package_ndc": "0009-0011-04", "marketing_start_date": "19550427"}], "brand_name": "Solu-Cortef", "product_id": "0009-0011_8512044a-4a54-4634-bb97-9e20126adc61", "dosage_form": "INJECTION, POWDER, FOR SOLUTION", "pharm_class": ["Corticosteroid Hormone Receptor Agonists [MoA]", "Corticosteroid [EPC]"], "product_ndc": "0009-0011", "generic_name": "hydrocortisone sodium succinate", "labeler_name": "Pharmacia & Upjohn Company LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Solu-Cortef", "active_ingredients": [{"name": "HYDROCORTISONE SODIUM SUCCINATE", "strength": "100 mg/2mL"}], "application_number": "NDA009866", "marketing_category": "NDA", "marketing_start_date": "19550427", "listing_expiration_date": "20261231"}